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5J73

De novo design of protein homo-oligomers with modular hydrogen bond network-mediated specificity

5J73 の概要
エントリーDOI10.2210/pdb5j73/pdb
分子名称protein design 2L4HC2_9 (2 entities in total)
機能のキーワードrosetta, de novo design, de novo protein
由来する生物種synthetic construct
タンパク質・核酸の鎖数4
化学式量合計37910.74
構造登録者
主引用文献Boyken, S.E.,Chen, Z.,Groves, B.,Langan, R.A.,Oberdorfer, G.,Ford, A.,Gilmore, J.M.,Xu, C.,DiMaio, F.,Pereira, J.H.,Sankaran, B.,Seelig, G.,Zwart, P.H.,Baker, D.
De novo design of protein homo-oligomers with modular hydrogen-bond network-mediated specificity.
Science, 352:680-687, 2016
Cited by
PubMed Abstract: In nature, structural specificity in DNA and proteins is encoded differently: In DNA, specificity arises from modular hydrogen bonds in the core of the double helix, whereas in proteins, specificity arises largely from buried hydrophobic packing complemented by irregular peripheral polar interactions. Here, we describe a general approach for designing a wide range of protein homo-oligomers with specificity determined by modular arrays of central hydrogen-bond networks. We use the approach to design dimers, trimers, and tetramers consisting of two concentric rings of helices, including previously not seen triangular, square, and supercoiled topologies. X-ray crystallography confirms that the structures overall, and the hydrogen-bond networks in particular, are nearly identical to the design models, and the networks confer interaction specificity in vivo. The ability to design extensive hydrogen-bond networks with atomic accuracy enables the programming of protein interaction specificity for a broad range of synthetic biology applications; more generally, our results demonstrate that, even with the tremendous diversity observed in nature, there are fundamentally new modes of interaction to be discovered in proteins.
PubMed: 27151862
DOI: 10.1126/science.aad8865
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.56 Å)
構造検証レポート
Validation report summary of 5j73
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-02-11に公開中

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